Canonical Allele Identifier: CA2320767974

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125465G= , CM000681.2:g.7125465G=	GRCh38
NC_000019.9:g.7125476G= , CM000681.1:g.7125476G=	GRCh37
NC_000019.8:g.7076476G=	NCBI36
NG_008852.2:g.173536C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3076C= MANE Select	ENSP00000303830.4:p.Leu1026=
ENST00000302850.9:c.3076C=	ENSP00000303830.4:p.Leu1026=
ENST00000341500.9:c.3040C=	ENSP00000342838.4:p.Leu1014=
NM_000208.2:c.3076C=	NP_000199.2:p.Leu1026=
NM_000208.3:c.3076C=	NP_000199.2:p.Leu1026=
NM_001079817.1:c.3040C=	NP_001073285.1:p.Leu1014=
NM_001079817.2:c.3040C=	NP_001073285.1:p.Leu1014=
XM_011527988.1:c.3151C=	XP_011526290.1:p.Leu1051=
XM_011527989.1:c.3115C=	XP_011526291.1:p.Leu1039=
XM_011527988.2:c.3073C=	XP_011526290.2:p.Leu1025=
XM_011527989.3:c.3037C=	XP_011526291.2:p.Leu1013=
NM_000208.4:c.3076C= MANE Select	NP_000199.2:p.Leu1026=
NM_001079817.3:c.3040C=	NP_001073285.1:p.Leu1014=